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prairie-willi
The endowment will serve to finance the clinical trial of an innovative therapy for patients with Fragile X Syndrome and the discovery and clinical development of new PDE-10 inhibitors for the treatment of Prader-Willi syndrome
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Central adrenal insufficiency is rare in adults with Prader-Willi Syndrome
Central adrenal insufficiency is rare in adults with Prader-Willi Syndrome https://www.tauli.cat/institut/wp-content/uploads/2020/04/8559-min-min_opt-1200x750.jpg 1080 675 Guillem Cebrian Guillem Cebrian https://www.tauli.cat/institut/wp-content/uploads/2020/02/IMG-1030-150x150.png
By: Guillem Cebrian
Prader-Willi syndrome (PWS) is a disease of uncommon genetic origin considered, however, the most common cause of genetic obesity. According to data extracted from the web portal of the Spanish SPW Association, this disease affects one in 15.000 newborns. A scientific article on this disease was recently published in The Journal of Clinical Endocrinology & Metabolism with the participation of several international researchers who are experts in this syndrome. Among them is Dr.…
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